微泡
间质细胞
生物
PI3K/AKT/mTOR通路
癌症研究
磷酸肌醇3激酶
蛋白激酶B
细胞生长
骨髓
结直肠癌
癌症
信号转导
细胞生物学
免疫学
小RNA
生物化学
基因
遗传学
作者
F. Richard Yu,Feng Wu,Guoyin Shang,Chao Yin
出处
期刊:Genomics
[Elsevier]
日期:2023-07-01
卷期号:115 (4): 110636-110636
被引量:3
标识
DOI:10.1016/j.ygeno.2023.110636
摘要
Colorectal cancer (CRC) is the fourth most frequently diagnosed cancer worldwide. Bone marrow stromal cells (BMSCs) play an essential role in tumor development by secreting exosomes. Scavenger receptor class A member 5 (SCARA5) is a newly identified tumor suppressor. This study aimed to investigate the effects of BMSCs-derived exosomes (BMSCs-Exos) on CRC development and to explore their regulatory mechanisms. BMSCs-Exos showed an oval-shaped, bilayer membrane structure. BMSCs-Exos inhibited growth and motility of CRC cells, while BMSCs-Exos with SCARA5 knockdown significantly promoted cell proliferation and movement. Exosomal SCARA5 also effectively suppressed colorectal tumor growth in mouse xenografts. Further analysis revealed that exosomal SCARA5 inhibited the phosphorylation of protein kinase B and phosphoinositide 3-kinase in both CRC cells and tumors. In conclusion, SCARA5 in BMSCs-Exos inhibited CRC progression by inactivating PI3K/Akt, thus suggesting the potential clinical application of SCARA5-containing BMSCs-Exos for CRC treatment.
科研通智能强力驱动
Strongly Powered by AbleSci AI